Dicarboxylic Aminoaciduria

Watchlist
Retrieved
2021-01-23
Source
Trials
Genes
Drugs

Dicarboxylicaminoaciduria is characterised by infantile-onset hypoglycaemia and hyperprolinaemia associated, in certain cases, with intellectual deficit.

Epidemiology

Less than 10 cases have been reported to date.

Etiology

Defects in renal and intestinal glutamate and aspartate transport were also reported, suggesting that anomalies of the EAAC1 transporter, involved in the transport of these two amino acids, are the underlying cause of this syndrome.